Dear Friends, Sorry to Announce a Genocide

Dear Friends, Sorry to Announce a Genocide: Dr. Naomi Wolf on the Pfizer “Confidential Report”

It's Really True: They Know They Are Killing the Babies

By Dr. Naomi Wolf

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Incisive analysis by Dr. Naomi Wolf, first published by Global Research on May 31, 2022

***

I’ve been silent for some weeks. Forgive me.

The truth is: I’ve been rendered almost speechless — or the literary equivalent of that — because recently I’ve had the unenviable task of trying to announce to the world that indeed, a genocide — or what I’ve called, clumsily but urgently, a “baby die-off” — is underway.

The WarRoom/DailyClout Pfizer Documents Research Volunteers, a group of 3000 highly credentialled doctors, RNs, biostatisticians, medical fraud investigators, lab clinicians and research scientists, have been turning out report after report, as you may know, to tell the world what is in the 55,000 internal Pfizer documents which the FDA had asked a court to keep under wraps for 75 years.

By court order, these documents were forcibly disclosed. And our experts are serving humanity by reading through these documents and explaining them in lay terms. You can find all of the Volunteers’ reports on DailyClout.io.

The lies revealed are stunning.

The WarRoom/DailyClout Volunteers have confirmed:

that Pfizer (and thus the FDA) knew by December 2020 that the MRNA vaccines did not work — that they “waned in efficacy” and presented “vaccine failure.” One side effect of getting vaccinated, as they knew by one month after the mass 2020 rollout, was “COVID.”

Pfizer knew in May of 2021 that 35 minors’ hearts had been damaged a week after MRNA injection — but the FDA rolled out the EUA for teens a month later anyway, and parents did not get a press release from the US government about heart harms til August of 2021, after thousands of teens were vaccinated. [See this]

Pfizer (and thus the FDA; many of the documents say “FDA: CONFIDENTIAL” at the lower boundary) knew that, contrary to what the highly paid spokesmodels and bought-off physicians were assuring people, the MRNA, spike protein and lipid nanoparticles did not stay in the injection site in the deltoid, but rather went, within 48 hours, into the bloodstream, from there to lodge in the liver, spleen, adrenals, lymph nodes, and, if you are a woman, in the ovaries. [See this]

Pfizer (and thus the FDA) knew that the Moderna vaccine had 100 mcg of MRNA, lipid nanoparticles and spike protein, which was more than three times the 30 mcg of the adult Pfizer dose; the company’s internal documents show a higher rate of adverse events with the 100 mcg dose, so they stopped experimenting with that amount internally due to its “reactogenicity” — Pfizer’s words — but no one told all of the millions of Americans who all got the first and second 100 mcg Moderna dose, and the boosters.

Pfizer skewed the trial subjects so that almost three quarters were female — a gender that is less prone to cardiac damage. Pfizer lost the records of what became of hundreds of their trial subjects.

In the internal trials, there were over 42,000 adverse events and more than 1200 people died. Four of the people who died, died on the day they were injected.

Adverse events tallied up in the internal Pfizer documents are completely different from those reported on the CDC website or announced by corrupted physicians and medical organizations and hospitals. These include vast columns of joint pain, muscle pain (myalgia), masses of neurological effects include MS, Guillain Barre and Bell’s Palsy, encephaly, every iteration possible of blood clotting, thrombocytopenia at scale, strokes, hemorrhages, and many kinds of ruptures of membranes throughout the human body.

The side effects about which Pfizer and the FDA knew but you did not, include blistering problems, rashes, shingles, and herpetic conditions (indeed, a range of blistering conditions oddly foreshadowing the symptoms of monkeypox).

The internal documents show that Pfizer (and thus the FDA) knew that angry red welts or hives were

#CIA-linked company manufactures #Moderna’s #COVID #booster shots

 by: Sara Middleton, staff writer | October 10, 2022

(NaturalHealth365)  Nearly three years into the pandemic, and it seems that another three-letter agency has joined the chat.

After witnessing the U.S. Food and Drug Administration (FDA), U.S. Centers for Disease Control and Prevention (CDC), World Health Organization (WHO), and others handle (and mishandle) the coronavirus pandemic, it seems that yet another major agency – strangely, the U.S. Central Intelligence Agency (CIA) – is at getting involved in vax production.

Moderna’s revamped vax being produced by new biotech company led by leaders with links to FDA, CIA

Pharmaceutical company Moderna, one of two companies responsible for the

CDC, FDA, Prueba Covid, Células Humanas, Virus del Resfriado Común

Los CDC y la FDA falsificaron el protocolo de prueba ‘Covid’ mediante el uso de células humanas mezcladas con fragmentos del virus del resfriado común – Dan Dicks

laverdadofende.blog 

En una impactante revelación reportada por primera vez por Dan Dicks de  Press for Truth  (Canadá) , un documento de la FDA admite que los CDC y la FDA conspiraron para fabricar un protocolo de prueba de covid-19 utilizando células humanas combinadas con fragmentos del virus del resfriado común porque  no tenían muestras físicas. del virus «covid» SARS-CoV-2  disponible.

Sin material de referencia físico para usar para la calibración y confirmación, la prueba no tiene ninguna base científica en la realidad física. Y todo el análisis de PCR basado en este protocolo es completamente fraudulento, marcando a las personas como «positivas» para covid cuando simplemente poseen pequeñas cantidades de fragmentos de ARN de otras cepas de coronavirus que circulan en su sangre.

El documento de la FDA, disponible  en el sitio web FDA.gov , se titula “Panel de diagnóstico de RT-PCR en tiempo real de los CDC 2019-Novel Coronavirus (2019-nCoV)”. El documento admite asombrosamente: (énfasis nuestro)

Dado que  no había aislados de virus cuantificados de 2019-nCoV disponibles para uso de los CDC en el momento en que se desarrolló la prueba  y se realizó este estudio, los ensayos diseñados para la detección del ARN de 2019-nCoV se probaron con cepas caracterizadas de ARN de longitud completa transcrito in vitro ( Gen N; acceso a GenBank: MN908947.2) de título conocido (copias de ARN / µl) añadido a un diluyente que consiste en una suspensión de células A549 humanas y  medio de transporte viral (VTM) para imitar la muestra clínica.Este video pronto será prohibido. Ver antes de que se elimineSecretos reveladosAnuncios de RevcontentMás información>

En otras palabras, no tenían virus covid a partir del cual desarrollar y calibrar la prueba, por lo que

#FDA Investigates #AllergicReactions to #Pfizer #COVIDVaccine After More #HealthcareWorkers #Hospitalized

Posted on:

Tuesday, December 22nd 2020 at 4:15 pm

Written By:

Children's Health Defense

Originally published on www.childrenshealthdefense.org

The FDA is investigating allergic reactions in "multiple states." The agency acknowledged the reactions may have been caused by PEG, a compound in the Pfizer vaccine that CHD previously told the FDA could put millions of people at risk.

The U.S. Food and Drug Administration (FDA) told reporters late Friday the agency is investigating "about five" allergic reactions to the Pfizer COVID-19 vaccine in "multiple states."

The announcement followed Friday's news that an Illinois hospital temporarily shut down its COVID vaccination program after four healthcare workers there experienced allergic reactions -- one of which was severe -- to the vaccine.

Also on Friday, CNN reported that a third healthcare worker in Alaska was hospitalized for six hours for an anaphylactic reaction to the Pfizer vaccine. The report came on the heels of last week's news that two Alaskan healthcare workers had severe allergic reactions -- including one woman who was hospitalized for at least two nights after going into anaphylactic shock.

Anaphylaxis is a severe, potentially life-threatening allergic reaction that can occur within seconds or minutes of exposure to something a person is allergic to. If not treated immediately, it can be fatal, the Mayo Clinic explains.

According to Reuters and other news reports, the director of the FDA's Center for Biologics Evaluation and Research, Dr. Peter Marks, said polyethylene glycol (PEG), a compound in the Pfizer and Moderna vaccines, may have triggered the allergic reactions in the U.S.

The Pfizer and newly approved Moderna vaccines contain PEG. Both vaccines were approved by the FDA for emergency use, but are not yet licensed.

Lyn Redwood, president of Children's Health Defense (CHD), said there shouldn't be any mystery at

#COVID19Vaccine #Bombshell: #FDA #Documents #Reveal #DEATH + 21 #SeriousConditions As Possible #AdverseOutcomes

Posted on:
Sunday, December 6th 2020 at 6:45 pm

Written By:

GMI Reporter

Public discussion and documents reveal that the FDA knows that rushed-to-market COVID-19 vaccines may cause a wide range of life-threatening side effects, including death.

Unless the public is made aware of their real effects, and is given a choice, their widespread coercive promotion as "safe and effective" and "necessary" violates the medical ethical principle of informed consent.

Act now via Stand for Health Freedom to stand up for your rights! 

A US Food & Drug Administration advisory committee meeting titled, “Vaccines and Related Biological Products,” presented online on October 22, 2020, included a 27 slide powerpoint presentation by Steve Anderson, PhD, MPP Director, Office of Biostatistics & Epidemiology, Center for Biologics Evaluation and Research (CBER). Slide 16 of his presentation included a “DRAFT Working list of possible adverse event outcomes” associated with the imminent rollout of COVID-19 vaccines subject to FDA safety surveillance, showing that death, as well as 21 other conditions (most of which are possibly life-threatening), are listed as possible adverse outcomes of the COVID-19

#FDA #Merck's #Ebola #Vaccine

FDA Approves Merck's New Live Ebola Vaccine Which It Says Can Shed and Cause Immunosuppression

Merck has received the FDA's fast-tracked approval of a live, genetically modified Ebola vaccine which, according to its vaccine insert, can cause a novel new form of Ebola-type infection, resulting in immunosuppression and possible shedding of live virus to others.

On Dec. 20th, 2019, Merck announced it received FDA approval for an Ebola vaccine which contains the virus known as recombinant vesicular stomatitis virus–Zaire Ebola virus (rVSV-ZEBOV), and will be marketed under the name ERVEBO.

The rVSV-ZEBOV is a live, replication-competent virus, produced with the same African green monkey derived Vero cell line Merck used to create the Rotateq vaccine targeting rotavirus infections. The Vero cell line has been previously identified to carry at least two surreptitious simian

New #HepatitisB #Vaccine Found To Massively Increase #HeartAttack Odds

vaxxter,com

The FDA recently approved a new hepatitis B vaccine, but it seems there is some trouble in vaccine paradise. According to a new study that MedPageToday reported earlier, the new vaccine is being implicated in causing myocardial infarction issues.

Via MedPagetoday.com

In the trial, an acute myocardial infarction occurred in 14 people in the Dynavax group, but in only one person receiving the conventional vaccine. The events were confirmed by adjudication. Since the Dynavax group was twice as large, the risk of acute myocardial infarction in the trial was seven times greater with the new vaccine. The FDA wants to know if the new vaccine should be approved for use in millions of people.

What do you say? What recommendation would you make?

If you think this is just hypothetical, think again. On July 28, 2017, the FDA convened a public advisory committee meeting to consider this exact question. The members of the committee consisted primarily of experts in infectious diseases and immunology. I was the only cardiologist on the committee.

If the 14:1 imbalance was due to the play of chance, then the issue of myocardial infarction risk was spurious, and the vaccine should be approved. However, if the 14:1 imbalance reflected a real increase in cardiovascular risk, then approval of Dynavax vaccine would be problematic.
Was it biologically plausible for the new vaccine to cause heart attacks?

The new adjuvant in the vaccine caused an inflammatory response (of uncertain duration), and inflammation is an important cause of rupture of atherosclerotic plaques. So a causal linkage was not out of the question.

#FDA’s #Banned #Vitamin May Hold Key To #Cure #Cancer

vaxxter,com

In the 1980’s, vitamin B17 was banned by the FDA. Many holistic medical practitioners strongly believe the vitamin to be an effective treatment for cancer. And to this day, the war over vitamin B17 and the controversy that has followed continues on. The vitamin can no longer be found on any shelves and though some in the medical community continue to exchange blows over its legitimacy, the general public is rather obtuse to its existence. Vitamin B17 is scientifically known as mandelonitrile beta-D-gentiobioside.

If you search vitamin B17 today, you’ll find both spectrums of the controversy well represented. Some detailing it’s dangers, others lending credence to its value and usefulness. The polarizing discourse usually leaves the Google researcher somewhat befuddled. There are many claims that vitamin B17 has cured cancer.

Vitamin B17 is also known as amygdalin or laetrile. It’s a glycoside nutrient that’s linked by many alternative health practitioners to cancer prevention. And many claim, as mentioned prior, that it has actually cured cancer.

Vitamin B17 works with vitamins A, C and E to eliminate toxic cells from the body. This is the starting point for vitamin B17’s legitimacy claim as a healer. Due to this, it is also said to strengthen the immune system.

Vitamin B17 is a nitriloside and naturally contains nitriloside. Laetrile is an extract form of B17 that is known to allegedly prevent cancer via a process of hydrogen cyanide production.

Vitamin B17 and Cancer
Many studies show that vitamin B17 is a strong treatment for cancer. These studies also show that

#CDC Forced to #Release Documents Showing They Knew #Vaccine Preservative Causes #Autism

PhD Scientist and Biochemist reveals Hidden CDC documents showing Thimerosal In Vaccines increase Neurologic problems 

tapnewswire,com 

The CDC has been shunning the correlations among thimerosal and neurological disorders for a totally long term. Despite the fact that the FDA gave a two year deadline to get rid of the mercury based preservative from vaccines after the neurotoxin was banned in 1999, it nonetheless remains to at the present time in 60 percentage of flu vaccines. A vaccine industry watchdog has now received CDC documents that display statistically tremendous dangers of autism associated with the vaccine preservative, something the CDC denies even if confronted with their very own information.

For nearly ten years, Brian Hooker has been soliciting for documents which might be kept under tight wraps through the facilities for disorder manipulate and Prevention (CDC). His greater than a hundred Freedom of records Act (FOIA) requests have led to copious evidence that the vaccine preservative Thimerosal, which continues to be used inside the flu shot this is administered to pregnant ladies and toddlers, can purpose autism and different neurodevelopmental disorders.

Dr. Hooker, a PhD scientist, worked with participants of Congress to craft the letter to the CDC that these days ended in his obtaining long-awaited facts from the CDC, the significance of that’s historic. 

According to Hooker, the facts on over four hundred,000 babies born among 1991 and 1997, which

Two More #MMRVaccine #Whistleblowers: They’re Suing

Two more MMR vaccine whistleblowers: they’re suing

by Jon Rappoport

Where there’s smoke and fire—there’s more fire.

You pro-vaccine soccer moms: pay attention.

“The bigger the lie, the bigger the truth it is concealing. The truth is what people are afraid to accept.” (The Underground, Jon Rappoport)

The censored film, Vaxxed (trailer), has escaped the claws of the “protectors of all truth.” It has been showing to packed houses all over the country. It relates the specific crime of scientific fraud at the CDC. A whistleblower, William Thompson, confesses that he and his CDC colleagues lied and cheated and omitted vital data, in order to give the MMR vaccine a free pass and claim it had no connection to autism—when it did have a connection.

That’s the purpose and meaning and focus of this astonishing film.

But there is more. There are other whistleblowers shining a light on the MMR (mumps, measles, rubella) vaccine. Specifically, the mumps component of the vaccine and its ineffectiveness.

The #FDA Admits It Uses #People As #GuineaPigs

 

by Gary TruthKings

Pharmaceutical companies act under an umbrella of protective immunity when it comes to Vaccines, but they are aggressive with almost all their medications. They fear hardly any repercussions for making “mistakes,” which often cost human lives. Because pharmaceutical companies fear little in the way of responsive litigation, they really act on their own free will. Part of that free will using people as their own guinea pigs for testing medications.

When it comes to medications, the typical protocol is to perform a series of safety test which, presumably, would lower the risk for people getting harmed by the medications. But often time those “test” are actually just the act of releasing them and “seeing how it goes.” Take an example from 2006, when the FDA forced Impax Laboratories to take Wellbutrin XL off the market. The reason? The FDA says that Wellbutrin XL simply did not work. But worse more? While it may sound as if the procedure worked perfectly, the fact is that Wellbutrin XL had been on the market, in a failed capacity, for 5 years. The FDA ignored a failed medication for 5 years.

The FDA approved the medication originally without any testing. The FDA assumed that if lower doses had worked, increased doses would work fine as well. In this scenario, people became the guinea pigs for

#FDA Panel Examines #Maternal #Vaccine

This is the worst thing I’ve read in some time. For years, pregnant women were advised to avoid aspirin or anti-histamines, not drink coffee or wine, or eat sushi. But now the FDA intends to examine the potential for what is being called “maternal vaccines.” And it’s as insane as it sounds. 

An advisory panel working on behalf of the FDA is exploring the use of maternal immunizations intended to “protect” infants from disease. The meeting was held in Silver Spring, Maryland. The FDA’s Vaccines and

#EU Agency Opens #Investigation into #HPV #Vaccine

After Shot Damages Thousands of Families

 tapnewswire,com

The European Medicines Agency (EMA) has launched a probe into the highly controversial HPV vaccination program following thousands of reports of young girls falling seriously ill after getting jabbed. Per the Swedish news source Svenska Dagbladet (SvD), the European Union’s version of the Food And Drug Administration (FDA) launched the investigation to determine whether or not the safety claims associated with Gardasil and Cervarix, the two HPV vaccines currently in circulation, are actually legitimate.

The multinational drug corporations behind the two vaccines, Merck & Co. and GlaxoSmithKline (GSK), respectively, say the vaccines are perfectly safe and come with minimal risk of side effects. But the many thousands of young girls throughout the world who’ve suffered serious side effects, including several hundred

#FDA is the New #Murder Inc

Dead doctors, dead patients and corporate bullying: 

How FDA is the new Murder Inc

 

by: L.J. Devon, Staff Writer

(NaturalNews) When the US Food and Drug Administration (FDA) raided Dr. Jeffrey Bradstreet’s offices this year, they were determined to put an end to his research and use of Globulin component Macrophage Activating Factor (GcMAF) because this research was essentially making vaccines look like violent, mad science. (View the search warrant here) 

 

Globulin component, a protein naturally made by the body, normally binds with vitamin D to activate the acceleration of macrophages to destroy infection in the body. Dr. Bradstreet was finding out that when a person is injected with vaccine viruses, this natural binding process between globulin component and vitamin D is blocked by an enzyme called nagalase. Nagalase can be intentionally injected to wipe out the GcMAF protein facilities on the surface of one’s T and B lymphocytes, leaving the person with a compromised immune system. Did the FDA want to suppress this information? 

Before he suspiciously died, Dr. Bradstreet treated 1,100 patients with GcMAF with an astonishing 85 percent response rate. He also found out that the destructive enzyme nagalase was pervasive in fully

#Cancer #Enzyme being #Injected into #Kids in #Vaccines

tapnewswire.com

Renown holistic doctor found dead one week after FDA raids clinic

This seems to be the case with Dr. James Jeffrey Bradstreet, who was recently found dead after his body was discovered floating in a North Carolina river with a single gunshot wound to the chest. Bradstreet, a renowned physician known for his skepticism of immunizations (particularly the MMR vaccine), and his progressive autism research, was raided by the FDA one week before his mysterious death. The details of the raid remain largely unknown. 

Personally affected by autism, as both his son and stepson were diagnosed with the condition, a significant portion of Dr. Bradstreet’s work was dedicated to this cause. He even testified twice before the U.S House of Representatives about the link between vaccines and autism. 

As Natural News‘ reported, leading up to his death, Dr. Bradstreet was working with a little-known molecule that occurs naturally in the human body. GcMAF (Globulin component Macrophage Activating Factor), which is the GC protein after it combines with vitamin D in the body, has the potential to be a universal cure for cancer. 

It’s also believed to be capable of treating and reversing autism, HIV, liver/kidney disease and diabetes.

5 Most Horrifying Things About Monsanto

To read the complete article, please visit: http://www.alternet.org/take-action/5-most-horrifying-things-about-monsanto-why-you-should-join-global-movement-and-protest?page=0%2C1

 

1. Profiteering poisonous chemical company posing as agribusiness.

Remember the horrors of Operation Ranch Hand during the Vietnam War, when the US military designed a chemical warfare program and used the herbicide and defoliant Agent Orange to kill and maim 400,000 people (estimated by the Vietnam government), and ultimately cause birth defects for 500,000 children? Monsanto made that possible.

Monsanto began as a chemical company in 1901 and was responsible for some of the most damaging toxins in US history, like polychlorinated biphenyls (PCB’s), and dioxin. Consumer advocacy group Food and Water Watch (FWW) released a report on APril 3 detailing Monsanto’s role in chemical disasters, Agent Orange, and the first genetically modified plant cell. The report shows that the “feed-the-world” agricultural and life sciences company Monsanto markets itself as today is only a recent development. The majority of Monsanto’s history is involved with heavy industrial chemical production, including the supply of Agent Orange to the US for Vietnam operations from 1962-'71.

2. Building a monopoly, putting farmers out of work.

There is nothing more quintessentially American than the independent family farmer; and there is nothing more un-American than stomping out that farmer’s livelihood to bolster your corporate monopoly. Monsanto is attempting this as it sues small farmers out of their livelihoods time and again.

You might have heard about the 75-year-old soybean farmer from Indiana, Vernon Hugh Bowman, who was ordered in the beginning of May to pay Monsanto $85,000 in damages for using second-generation seeds genetically modified with Monsanto’s pesticide resistant “Roundup Ready,” treatment. He pulled the seeds from the local grain elevator, which is usually used for feed crop, and planted them. The court decided Monsanto’s patent extends even to the offspring of its seeds, and the farmer had violated the company’s patent.

3. Controlling the food, privatizing the water.

Half of the Earth’s population will live in an area with significant water stress by 2030, according to estimates from the Organization for Economic Cooperation & Development. Corporations like Monsanto (along with Royal Dutch Shell and Nestle) are vying for a future in which free water supply is a thing of the past, and private companies control public water sources.

According to a government report titled " Intelligence Community Assessment; Global Water Security," by 2025, the world's population will likely exceed 8 billion people, and the demand for water will be 40 percent higher than sustainable water supplies available, with water needs of around 6,900 billion cubic meters due to population growth.

4. Running the FDA, writing its own protection laws.

Ex-Monsanto executives run the United States Food and Drug Administration, the agency tasked with ensuring food safety for the American public.

This obvious conflict of interest could explain the lack of government-led research on the long-term effects of GM products. Recently, the U.S. Congress and president together passed the law that has been dubbed “Monsanto Protection Act.” Among other things, the new law bans courts from halting the sale of Monsanto’s genetically modified seeds.

5. Continuing environmental nightmares.

As Tami Canal points out, studies have linked Monsanto and other biotech conglomerates to the decline of bee colonies in the US and abroad.

Their environmental blunders don’t stop there. In 2002 the Washington Post published a piece titled “ Monsanto Hid Decades of Pollution,” outlining the corporation’s pollution of an Alabama town with toxic PCBs for decades without disclosure.